Kohzuki M, Hodsman G P, Harrison R W, Western P S, Johnston C I
Melbourne University Department of Medicine, Austin Hospital, Heidelberg, Victoria, Australia.
J Cardiovasc Pharmacol. 1989;13 Suppl 6:S43-6.
The natriuretic, diuretic, and hypotensive responses to infused atrial natriuretic peptide (ANP) were measured in rats 4 weeks after myocardial infarction induced by coronary artery ligation. Rat [1-28]-ANP was infused intravenously in doses of 0.1, 0.3, and 1.0 microgram/kg/min for 30 min each under pentobarbital anesthesia. There was a marked natriuresis, diuresis, and fall in blood pressure in rats with infarction but each response was significantly attenuated when compared with sham-operated controls (ANOVA: p less than 0.01, p less than 0.05, and p less than 0.01, respectively). Urinary cyclic guanosine monophosphate (cGMP) excretion in rats with infarction was higher than that of controls but rose to the same absolute level in both groups in response to ANP infusion (0.3 microgram/kg/min). Reduced ANP responsiveness may result from impaired postreceptor mechanisms or from physiological antagonism by angiotensin II. Reduced ANP responsiveness may partly explain impaired salt handling in heart failure.
在冠状动脉结扎诱导心肌梗死后4周的大鼠中,测量了对静脉输注心房利钠肽(ANP)的利钠、利尿和降压反应。在戊巴比妥麻醉下,以0.1、0.3和1.0微克/千克/分钟的剂量静脉输注大鼠[1-28]-ANP,每次持续30分钟。梗死大鼠出现明显的利钠、利尿和血压下降,但与假手术对照组相比,每种反应均明显减弱(方差分析:p分别小于0.01、p小于0.05和p小于0.01)。梗死大鼠的尿中环磷酸鸟苷(cGMP)排泄量高于对照组,但在输注ANP(0.3微克/千克/分钟)后,两组的绝对水平上升至相同。ANP反应性降低可能是由于受体后机制受损或血管紧张素II的生理拮抗作用所致。ANP反应性降低可能部分解释了心力衰竭时盐处理受损的原因。